Relevant bibliographies by topics / 2-amino benzamide

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  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic '2-amino benzamide'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "2-amino benzamide"

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Kushwaha, Mr Abhay, Dr Shailesh Jain, Mr Ajay Kumar, Mr Ritesh Raj, Dr Phool Singh Yaduwanshi, and Dr Dhanraj Patidar. "An Overall Review of Different Derivatives That Activate Glucokinase Enzyme Having Multiple Actions to Treat Type 2 Diabetes." International Journal of Pharmaceutical Research and Applications 10, no. 1 (2025): 358–67. https://doi.org/10.35629/4494-1001358367.

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Different derivatives like3,6-disubstituted2- pyridine carboxamide derivatives, Phenylethyl benzamide derivatives, Carboxypyridine benzamide derivatives, Pyrazole benzamide derivatives, Quinazoline-2,4 dione analogs, Ketopiperazine analogs, Cycloalkyl-fused Nthiazol-2-yl-benzamides derivatives, 1,4- disubstituted indazoles derivatives, 2,5,6- trisubstituted indole derivatives, Azaindole derivatives andPyrimidone derivatives was designed, synthesized and evaluated the pharmacological activity in mice. Such compounds activate the glucokinase by interaction between glucokinase activators and gluc
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Journal, Baghdad Science. "Synthesis of New Amide and ThioUrease Compounds." Baghdad Science Journal 4, no. 3 (2007): 430–37. http://dx.doi.org/10.21123/bsj.4.3.430-437.

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The reaction of some new Schiff bases ( 2-[(2-Amino – ethylimino)-methyl]-R , 2-({2-[(R-benzylidene)-amino]-ethylimino}-methyl)-R with Benzoyl chloride or Acetyl chloride were carried out. Subsequent reactions of these products N-(2-Amino-ethyl)-N-[Chloro-(R) –methyl]-benzamide or N-(2-{?-[chloro-(R) –methyl]-amino}-ethyl)-N-[chloro-(R) –methyl]- benzamide with thiourea afforded thioureas compounds. The synthesized compounds were confirmed by their IR,UV,spectra and C.H.N. analysis.
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Garg, Ajay Kumar, Ranjan Kumar Singh, Vaibhav Saxena, Saurabh Kr Sinha, and Sanjay Rao. "Synthesis, Characterization, and Anti-inflammatory activity of Some Novel Oxazole Derivatives." Journal of Drug Delivery and Therapeutics 13, no. 1 (2023): 26–28. http://dx.doi.org/10.22270/jddt.v13i1.5719.

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A series of novel oxazole derivatives (A, A1, A2) were synthesized starting from acetone and urea. The compound (A) was obtained by heating it with acetophenone and urea in iodine. Compound (A) on treatment with 4-amino benzaldehyde (Z)-N-(4-amino benzylidine)-4-((E)-Penta-2, 4-diene-2) oxazole-2-amine afforded (A1). Acylation of compound (A) with 4-amino benzoyl chloride to obtain the corresponding N-(4 phenyl oxazole-2- yl)- benzamide (A2). The structures of compounds have been established employing FTIR and 1H-NMR spectral analysis. All oxazole derivatives were evaluated for anti-inflammato
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Pokotylo, Ihor O., Pavlo V. Zadorozhnii, Vadym V. Kiselev, Oxana V. Okhtina, and Aleksandr V. Kharchenko. "Some New Heterocyclisations Based on N-(2,2-dichloro-1-isothiocyanatoethyl)benzamide Derivatives." Acta Chemica Iasi 27, no. 1 (2019): 65–72. http://dx.doi.org/10.2478/achi-2019-0005.

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Abstract Based on the readily available N-(2,2-dichloro-1-(2-(4-methylbenzoyl)-hydrazine-1-carbothioamido)ethyl)benzamide, the corresponding N-(2,2-dichloro-1-((5-(p-tolyl)-1,3,4-oxadiazol-2-yl)amino)ethyl)benzamide and 5-(p-tolyl)-1,3,4-thiadiazol-2-amine were obtained. The products were received in acceptable yields and were isolated from the reaction mixture without any particular difficulty. The structure of the compounds obtained was confirmed by 1H, 13C NMR spectroscopy and mass spectrometry data.
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Selvakumaran, N., R. Karvembu, Seik Weng Ng, and Edward R. T. Tiekink. "3-({[Bis(2-methylpropyl)carbamothioyl]amino}carbonyl)benzamide." Acta Crystallographica Section E Structure Reports Online 69, no. 7 (2013): o1183. http://dx.doi.org/10.1107/s1600536813017455.

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Gaston, Lewis A., Martin A. Locke, Steven C. Wagner, Robert M. Zablotowicz, and Krishna N. Reddy. "Sorption of Bentazon and Degradation Products in Two Mississippi Soils." Weed Science 44, no. 3 (1996): 678–82. http://dx.doi.org/10.1017/s0043174500094522.

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Bentazon degradation in soil typically proceeds with development of bound residue. Low sorption of bentazon suggests that this residue consists of degradation products; however, there is little data on the sorption behavior of these products. This study was undertaken to determine the sorption of bentazon and the degradation products 2-amino-N-isopropyl benzamide, 2-aminobenzoic acid, andN-methyl bentazon in Dundee silt loam and Sharkey clay, two common agricultural soils of the Mississippi Delta. Greater sorption of bentazon and degradation products in the Sharkey soil was related to finer te
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Konovalova, S. A., A. P. Avdeenko, V. I. Lubenets, O. Z. Komarovska-Porokhnyavets, I. Yu Yakymenko, and E. N. Lysenko. "BIOLOGICAL ACTIVITY OF N-{3-[(4-METHYLBENZENE-1- SULFONYL)IMINO]-6-OXOCYCLOHEXA-1,4-DIEN-1-YL}ARYLAMIDES AND THEIR DERIVATIVES." Odesa National University Herald. Chemistry 26, no. 1(77) (2021): 37–47. http://dx.doi.org/10.18524/2304-0947.2021.1(77).226136.

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N-{3-[(4-Methylbenzene-1-sulfonyl)imino]-6-oxocyclohexa-1,4-dien-1-yl}arylamides and their derivatives were synthesized by the reaction of the corresponding N-(4-oxocyclohexa-2,5-dien-1-ylidene)arylsulfonamides with N-chloramides. The biological activity of the synthesized compounds was studied on test cultures of Escherichia coli 67, Staphylococcus aureus 209-p, Mycobacterium luteum VKM B-868 and fungi Candida tenuis VKM Y-70, Aspergillus niger VKM F-1119 by the method of diffusion of substances into agar on a solid nutrient medium. The degree of activity of the test compounds was determined
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Belz, Tyson, Saleh Ihmaid, Jasim Al-Rawi, and Steve Petrovski. "Synthesis Characterization and Antibacterial, Antifungal Activity of N-(Benzyl Carbamoyl or Carbamothioyl)-2-hydroxy Substituted Benzamide and 2-Benzyl Amino-Substituted Benzoxazines." International Journal of Medicinal Chemistry 2013 (October 31, 2013): 1–20. http://dx.doi.org/10.1155/2013/436397.

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New N-(benzyl carbamothioyl)-2-hydroxy substituted benzamides 13, 20, and 21 were synthesized using sodium bicarbonate and benzyl amine with 2-thioxo-substituted-1,3-benzoxazines 6, 10a, b, 11c, and 12a–n. The 2-thioxo-substituted-1,3-oxazines 6, 10a-b, 11d 12a–n, and 26 were converted to the corresponding 2-methylthio-substituted-1,3-oxazines 14a–l and 24 which were then converted to 2-benzyl amino-substituted-benzoxazines 15a–i by refluxing with benzylamine. Products 15a, b, e, f, and g were also synthesized by boiling the corresponding N-(benzyl carbamothioyl)-2-hydroxy substituted benzamid
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Zhang, Yan, Jian-Quan Liu, and Xiang-Shan Wang. "An efficient synthesis of 16H-dibenzo[2,3:6,7][1,4]oxazepino[5,4-b]quinazolin-16-ones via an Ullmann reaction catalyzed by CuI." Organic & Biomolecular Chemistry 16, no. 10 (2018): 1679–85. http://dx.doi.org/10.1039/c8ob00005k.

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16H-Dibenzo[2,3:6,7][1,4]oxazepino[5,4-b]quinazolin-16-ones were obtained from the available reactants 2-amino-N-(2-hydroxyphenyl)benzamide and 2-bromobenzaldehyde via an Ullmann reaction catalyzed by CuI.
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Haller, Joseph P., Warunee Thaenghin, Wannipa Un-chai, and Kenneth J. Haller. "Inductive and supramolecular effects in 2-amino-N-(2-hydroxyphenyl)benzamide." Acta Crystallographica Section A Foundations and Advances 73, a2 (2017): C685. http://dx.doi.org/10.1107/s205327331708888x.

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Dissertations / Theses on the topic "2-amino benzamide"

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Delamare, Madeleine. "Nouvelles voies de synthèse d'hétérocycles polyazanaphtalènes en vue de leur application en pharmacie, en agro-industrie et en phytochimie." Rouen, 1998. http://www.theses.fr/1998ROUES024.

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L'activité de produits imidazolés vis-à-vis de l'inhibition de la farnésyl transférase a conduit au développement d'un programme de recherche industriel ayant pour base d'une part un azole et d'autre part un hétérocycle permettant une reconnaissance enzymatique spécifique. Dans le cadre de ce programme, nous nous sommes intéressés aux synthèses de divers hétérocycles de structures polyazanaphtalènes. Ainsi, des 6-acylisoquinol-1(2H)-ones, des 6- et 7-formyl-1,8-naphtyridin-2-ones et des 6- et 7-formyl-1,5-naphtyridin-2-ones, pouvant être substituées en position 3 par un groupe méthyle et en po
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Marquezin, Cássia Alessandra. "Técnicas de fluorescência no monitoramento de membranas modelo." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/59/59135/tde-26032009-154339/.

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Apresentamos os resultados de estudos sobre a utilização de técnicas baseadas no fenômeno de fluorescência para a investigação de processos relacionados a membranas modelo. Nessa investigação, estão envolvidas medidas de propriedades espectrais de absorção e emissão de luz por cromóforos adequados, determinação xperimental de perfis de decaimento temporal da fluorescência e correlação temporal de emissão fluorescente, bem como a utilização apropriada de metodologias para análise e interpretação dos dados experimentais. Foram utilizados diversos compostos que apresentam absorção e emissão na re
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Book chapters on the topic "2-amino benzamide"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex of 2-amino-N-(2′-carboxyphenyl)benzamide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_673.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of bis[2-amino-N-(2′-carboxyphenyl)-benzamido]ruthenium(III) bromide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_260.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 2-amino-4-benzamido-thiosemicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_254.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 2-amino-4-benzamido-thiosemicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_532.

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Hedden, David, D. Max Roundhill, Bruce N. Storhoff, and M. Brian Arnold. "Hybrid Tertiary Phosphine Amine and Amide Chelate Ligands: N -[2-(Diphenylphosphino)-Phenyl]Benzamide and 2-(Diphenylphosphino)-N -Phenylbenzamide." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132586.ch64.

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Houssine Mabrouk, El. "Synthesis and Characterization of New Racemic α-Heterocyclic α,α-Diaminoester and α,α-Diamino Acid Carboxylic: 2-Benzamido-2-[(Tetrahydro-Furan-2-Ylmethyl)Amino]Acetate and 2-Benzamido-2-[(Tetrahydro-Furan-2-Ylmethyl)Amino] Acetic Acid." In Furan Derivatives - Recent Advances and Applications. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.98408.

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We reported here the synthesis of new α,α-diaminoester and α,α-diamino acid derivatives, as 2-benzamido-2-[(tetrahydro-furan-2-ylmethyl)amino] acetic acid through alkaline hydrolysis reaction of corresponding N-benzoylated methyl α,α-diamino ester. The α,α-diaminoester derivative was synthesized by nucleophilic substitution of methyl α-azido glycinate N-benzoylated with 2-tetrahydrofuran-2-ylmethan-amine. The structure of these products were established on the basis of NMR spectroscopy (1H, 13C), and MS data.
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Döpp, H., and D. Döpp. "Cyclization of 2-[(ω-Hydroxyalkyl)amino]benzamides with Tris(diethylamino)phosphine." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00527.

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Taber, Douglass. "The Overman Syntheses of Nankakurines A and B." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0102.

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The tetracyclic alkaloids Nankakurine A and Nankakurine B were isolated from the club moss Lycopodium hamiltonii. A preliminary study of the biological activity of Nankakurine A suggested that it could induce secretion of neurotrophic factors and promote neuronal differentiation. The key step in the first syntheses of Nankakurine A and of Nankakurine B, reported (J. Am. Chem. Soc. 2008, 130, 11297) by Larry E. Overman of the University of California, Irvine was the intriguing intramolecular aza-Prins cyclization of 1 to 2. The starting material for the synthesis was 5-methyl cyclohexenone 6, p
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Taber, Douglass F. "Organic Functional Group Protection." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0012.

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Masato Kitamura of Nagoya University investigated (Chemistry Lett. 2009, 38, 188) the Ru-mediated deprotection of allyl ethers such as 1. The same catalyst was effective for the preparation of allyl ethers from the alcohol 2 and allyl alcohol. István E. Markó of the Université Catholique de Louvain showed (Organic Lett. 2009, 11, 2752) that SmI2 effected the reductive cleavage of an aryl ester 3, liberating the alcohol 4. Osamu Onomura of Nagasaki University found (Tetrahedron Lett. 2009, 50, 1466) that catalytic CuCl2 mediated the selective monoallylation of symmetrical diols such as 5. Péter
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Bhovi, Venkatesh K. "Synthesis and Characterization of Transition Metal(II) Complexes Derived from (E)-N-(4-Methylbenzylidene)-2-((Z)-(4-Methylbenzylidene) Amino)Benzamides: Investigation of Biological Activities." In Recent Developments in Chemistry and Biochemistry Research Vol. 3. B P International, 2024. http://dx.doi.org/10.9734/bpi/rdcbr/v3/419.

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Conference papers on the topic "2-amino benzamide"

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Nikalje, Anna Pratima, Shailee Tiwari, Sumaiya Siddiqui, and Julio Seijas Vázquez. "Microwave-assisted Facile Synthesis And Anticancer Evaluation Of N-((5-(substituted Methylene Amino)- 1,3,4-thiadiazol-2-yl)methyl) Benzamide Derivatives." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a010.

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Pavlova, Valeriia V., Pavlo V. Zadorozhnii, Vadym V. Kiselev, and Aleksandr V. Kharchenko. "Synthesis, Spectral Characteristics, and Molecular Docking Studies of 2,4-Dichloro-N-(2,2,2-trichloro-1-((5-(phenylamino)-1,3,4-thiadiazol-2-yl)amino)ethyl)benzamide." In ECSOC 2022. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13642.

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Gheysen, D., L. Piérard, P. Jacobs, H. R. Lijnen, A. Bollen, and D. Collen. "PROPERTIES OF A HUMAN RECOMBINANT FUSION PROTEIN OF THE ‘FINGER’ DOMAIN OF TISSUE-TYPE PLASMINOGEN ACTIVATOR (t-PA) AND A TRUNCATED SINGLE CHAIN UROKINASE-TYPE PLASMINOGEN ACTIVATOR (scu-PA)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643941.

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A hybrid between human tissue-type plasminogen activator (t-PA) and human single chain urokinase-type plasminogen activator (scu-PA) was obtained by ligation of cDNA fragments encoding the NH2-terminal amino acids 1 to 67 of t-PA and the COOH-ter-minal amino acids 136 to 411, of scu-PA. Both this chimaeric cDNA and cDNA encoding scu-PA were expressed in a mammalian system (HAK-cells) using bovine papilloma virus (BPV) derived vectors. Two stable cell lines were obtained which secreted the recombinant hybrid and the scu-PA at 1 μg/ml and 2 μg/ml u-PA related antigen respectively into the cultur
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Takeya, H., S. Kawabata, T. Miyata, T. Morita, and S. Iwanaga. "A MODIFIED METHOD FOR PURIFICATION OF BOVINE FACTOR VII AND ITS PRIMARY STRUCTURE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643785.

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A modified method for purification of factor VII from bovine plasma was developed. The isolation procedures consisted of four steps with the ordinary barium citrate adsorption (1), DEAE-Sepharose chromatography (2), twice chromatographies on a benzamidine-Sepharose column (3) and affinity chromatography on Affigel-10 coupled with staphylocoagulase produced by Staphylococcus aureus, strain 213 (4). This final step was very effective for the removal of prothrombin contained in the pooled fraction of factor VII. Thus, these procedures allowed higher recovery of factor VII than the earlier methods
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